Evidence map›Paper›PMID 42183859›Full record

ReviewNaunyn-Schmiedeberg's archives of pharmacology2026

Datopotamab deruxtecan for endocrine-resistant HR-positive/HER2-negative breast cancer: biological rationale and clinical evidence.

Bhargavi Gumma, Lohitha Gumma

Abstract readReview
PubMed Publisher
In one paragraph

Review in Naunyn-Schmiedeberg's archives of pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Bhargavi GummaJai Soorya Potti Sreeramulu Government Homeopathy Medical College, Ramanthapur, Hyderabad, 500013, Telangana, India.
Lohitha GummaDepartment of Pharmacy Practice, Chalapathi Institute of Pharmaceutical Sciences (Autonomous) Lam, Guntur, 522034, Andhra Pradesh, India. gummalohitha1902@gmail.com.ORCID http://orcid.org/0009-0002-5196-8081

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR-positive/HER2-negative) breast cancer is primarily managed with endocrine-based therapies; however, resistance to endocrine therapy and CDK4/6 inhibitors commonly develops in advanced disease. Following treatment failure, therapeutic options are largely limited to sequential chemotherapy, which provides modest clinical benefit and is associated with cumulative toxicity. Antibody-drug conjugates (ADCs) targeting trophoblast cell surface antigen 2 (TROP-2) have emerged as a promising strategy for delivering cytotoxic agents selectively to tumor cells in endocrine-refractory disease. This narrative review summarizes current evidence on the biological rationale, pharmacologic characteristics, and clinical development of datopotamab deruxtecan (Dato-DXd), with emphasis on findings from the phase III TROPION-Breast01 trial and relevant translational studies. Datopotamab deruxtecan is a TROP-2-directed ADC that enables targeted delivery of a potent topoisomerase I inhibitor payload to tumor cells. In the TROPION-Breast01 trial, Dato-DXd demonstrated a statistically significant improvement in progression-free survival compared with investigator's choice chemotherapy in patients with endocrine-refractory HR-positive/HER2-negative metastatic breast cancer. Clinical activity was observed across heterogeneous TROP-2 expression, including in heavily pretreated patients and those with visceral disease. Hematologic toxicity was relatively limited, although interstitial lung disease remains an important safety consideration requiring proactive monitoring. Datopotamab deruxtecan represents a clinically meaningful therapeutic option based on the targeted delivery of cytotoxic chemotherapy for patients with endocrine-resistant HR-positive/HER2-negative breast cancer. Ongoing studies are required to define optimal treatment sequencing, combination strategies, and long-term safety outcomes.

Indexed as

Antineoplastic AgentsBreast NeoplasmsImmunoconjugatesAnimalsAntigens, NeoplasmCell Adhesion MoleculesDrug Resistance, NeoplasmErb-b2 Receptor Tyrosine KinasesFemaleHumansAntigens, NeoplasmAntineoplastic AgentsCell Adhesion MoleculesERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesImmunoconjugatesTACSTD2 protein, humanDatopotamab deruxtecanHR-positive/HER2-negative metastatic breast cancerMetastatic breast cancerTROP2 antibody–drug conjugateTROPION-Breast01

Identifiers

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.